Formation of 1,4,2-Dithiazolidines or 1,3-Thiazetidines from 1,1-Dichloro-2-nitroethene and Phenylthiourea Derivatives

Yian Feng; Minming Zou; Runjiang Song; Xusheng Shao; Zhong Li; Xuhong Qian

doi:10.1021/acs.joc.6b01307

Formation of 1,4,2-Dithiazolidines or 1,3-Thiazetidines from 1,1-Dichloro-2-nitroethene and Phenylthiourea Derivatives

Yian Feng
, Minming Zou
, Runjiang Song
, Xusheng Shao^*
, Zhong Li
, Xuhong Qian

^*此作品的通讯作者

East China University of Science and Technology
Shanghai Collaborative Innovation Center for Biomanufacturing (SCICB)

科研成果: 期刊稿件 › 文章 › 同行评审

17 引用（Scopus）

摘要

A method for preparation of 1,4,2-dithiazolidine or 1,3-thiazetidine heterocycles was developed by reactions of phenylthioureas with 1,1-dichloro-2-nitroethene. The solvent has a significant influence on the type of product formation. 1,4,2-Dithiazolidines were formed in the aprotic solvent chloroform, while in the protic solvent ethanol, 1,3-thiazetidines were the main products.

源语言	英语
页（从-至）	10321-10327
页数	7
期刊	Journal of Organic Chemistry
卷	81
期	21
DOI	https://doi.org/10.1021/acs.joc.6b01307
出版状态	已出版 - 4 11月 2016
已对外发布	是

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title = "Formation of 1,4,2-Dithiazolidines or 1,3-Thiazetidines from 1,1-Dichloro-2-nitroethene and Phenylthiourea Derivatives",

abstract = "A method for preparation of 1,4,2-dithiazolidine or 1,3-thiazetidine heterocycles was developed by reactions of phenylthioureas with 1,1-dichloro-2-nitroethene. The solvent has a significant influence on the type of product formation. 1,4,2-Dithiazolidines were formed in the aprotic solvent chloroform, while in the protic solvent ethanol, 1,3-thiazetidines were the main products.",

author = "Yian Feng and Minming Zou and Runjiang Song and Xusheng Shao and Zhong Li and Xuhong Qian",

note = "Publisher Copyright: {\textcopyright} 2016 American Chemical Society.",

year = "2016",

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day = "4",

doi = "10.1021/acs.joc.6b01307",

language = "英语",

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T1 - Formation of 1,4,2-Dithiazolidines or 1,3-Thiazetidines from 1,1-Dichloro-2-nitroethene and Phenylthiourea Derivatives

AU - Feng, Yian

AU - Zou, Minming

AU - Song, Runjiang

AU - Shao, Xusheng

AU - Li, Zhong

AU - Qian, Xuhong

PY - 2016/11/4

Y1 - 2016/11/4

N2 - A method for preparation of 1,4,2-dithiazolidine or 1,3-thiazetidine heterocycles was developed by reactions of phenylthioureas with 1,1-dichloro-2-nitroethene. The solvent has a significant influence on the type of product formation. 1,4,2-Dithiazolidines were formed in the aprotic solvent chloroform, while in the protic solvent ethanol, 1,3-thiazetidines were the main products.

AB - A method for preparation of 1,4,2-dithiazolidine or 1,3-thiazetidine heterocycles was developed by reactions of phenylthioureas with 1,1-dichloro-2-nitroethene. The solvent has a significant influence on the type of product formation. 1,4,2-Dithiazolidines were formed in the aprotic solvent chloroform, while in the protic solvent ethanol, 1,3-thiazetidines were the main products.

UR - https://www.scopus.com/pages/publications/84994607994

U2 - 10.1021/acs.joc.6b01307

DO - 10.1021/acs.joc.6b01307

M3 - 文章

AN - SCOPUS:84994607994

SN - 0022-3263

VL - 81

SP - 10321

EP - 10327

JO - Journal of Organic Chemistry

JF - Journal of Organic Chemistry

IS - 21

ER -

Formation of 1,4,2-Dithiazolidines or 1,3-Thiazetidines from 1,1-Dichloro-2-nitroethene and Phenylthiourea Derivatives

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